Reactive amino-quinones, copolymers thereof and corrosion resistant information storage devices

ABSTRACT

Reactive aminoquinones of formula I or II ##STR1## wherein R is hydrogen, branched, linear or cyclic C 1  -C 6  alkyl, aralkyl, or phenyl which may be substituted by linear, branched or cyclic C 1  -C 4  alkyl, --NO 2 , F, OR 2 , NR 3   2 , wherein R 2  and R 3  are linear, branched or cyclic C 1  -C 6  alkyl, aralkyl or phenyl, 
     R 1  is a linear, branched or cyclic C 2  -C 18  alkylene chain, phenylene, aralkylene, alkarylene, or --(CH 2  CH 2  --O) n  --CH 2  --CH 2  --, wherein n is an integer from 1 to 50, 
     X is hydroxy, epoxy, vinyl, vinyloxy, acrylate, methacrylate or acylchloro 
     Y is N or CH; and 
     R 4  is linear or branched C 1  -C 6  alkyl which are useful in forming copolymers to prepare corrosion resistant binder compositions for magnetic information storage media, the copolymers formed, the magnetic information storage media and a method for improving corrosion resistance in magnetic particles are provided.

This application is a Division of application Ser. No. 08/019,917, filed on Feb. 19, 1993, now abandoned.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to reactive aminoquinones, copolymers containing them and use of these copolymers as corrosion resistant binders in information storage devices.

2. Discussion of the Background

Flexible magnetic information storage media have become one of the principle means of storing information over the last two decades. This is primarily because such information storage media are permanent and versatile and have a high storage capacity. Additionally, the information stored on these types of devices can be easily erased and the device used repeatedly.

During the last two decades, the flexible magnetic recording industry has striven to increase the information storage capacity for various magnetic information storage media, with metal particle tape and magnetooptic discs emerging as leading candidates. However, recent reports of corrosion problems for metal particle tape have been cause for considerable concern in the industry (D. Speliotis IEEE Trans. Magnetics 1990, 26(1) 124-126; D. Speliotis, Symposium on Corrosion of Electronic Materials and Devices, Electrochemical Society, Seattle, Wash. October 1990). Recent attempts to improve corrosion resistance in metal particle tape have used variants of metal particle tape which contain ceramic coated iron particles (Y. Yamamoto, K. Sumiya, A. Miyake, M. Kishimoto, and T. Taniguchi, IEEE Trans. Magnetics 1990, 26(5), 2098-2100). However, these have the drawback of being fragile and difficult to prepare using conventional methods. Thus, the issue of the reliability of metal particle tape, and magnetic recording media in general, due to iron particle corrosion remains unanswered.

One method of improving the corrosion resistance of metal particle based information storage media, would be to provide a coating for the metal particles which maintains the desirable characteristics of the information storage device, of flexibility, high capacity and product strength, while greatly improving the corrosion resistance and thus the lifetime of the device. However, until the discovery of the present invention, the above method has provided little improvement compared to the conventional polyurethane binder compositions used in magnetic information storage media.

SUMMARY OF THE INVENTION

Accordingly, one object of the present invention is to provide a reactive aminoquinone which can be incorporated into corrosion resistant binder compositions in information storage media.

Another object of the present invention is to provide a copolymer useful as a binder in information storage media, which contains as a constituent monomer a reactive aminoquinone, and which results in improved corrosion resistance of the magnetic particles in the device.

Another object is to provide an information storage device having improved corrosion resistance and improved mechanical properties.

These and other objects have been satisfied by the discovery of reactive aminoquinones of the formula I ##STR2## wherein R is hydrogen, branched, linear or cyclic C₁ -C₆ alkyl, aralkyl, or phenyl which may be substituted by linear, branched or cyclic C₁ -C₄ alkyl, --NO₂, F, OR², NR³ ₂, wherein R² and R³ are linear, branched or cyclic C₁ -C₆ alkyl, aralkyl or phenyl,

R¹ is a linear, branched or cyclic C₂ -C₁₈ alkylene chain, phenylene, aralkylene, alkarylene, or --(CH₂ CH₂ --O)_(n) --CH₂ --CH₂ --, wherein n is an integer from 1 to 50,

X is hydroxy, epoxy, vinyl aryl, vinyl, vinyloxy, acrylate, methacrylate or acylchloro or of the formula II ##STR3## wherein Y is N or CH R⁴ is linear or branched C₁ -C₆ alkyl and X is as defined above, their use in preparing copolymers useful as binders in information storage devices and information storage devices containing these copolymers as binders and having improved corrosion resistance and mechanical properties.

BRIEF DESCRIPTION OF THE FIGURES

A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying figure, wherein:

FIG. 1 is a graphical presentation of the corrosion results obtained with copolymers containing the reactive aminoquinones of the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention relates to reactive aminoquinone compounds of the formula I ##STR4## wherein R is hydrogen, branched, linear or cyclic C₁ -C₆ alkyl, aralkyl, or phenyl which may be substituted by linear, branched or cyclic C₁ -C₄ alkyl, --NO₂, F, OR², NR³ ₂, wherein R² and R³ are linear, branched or cyclic C₁ -C₆ alkyl, aralkyl or phenyl,

R¹ is a linear, branched or cyclic C₂ -C₁₈ alkylene chain, phenylene, aralkylene, alkarylene, or --(CH₂ CH₂ --O)_(n) --CH₂ --CH₂ --, wherein n is an integer from 1 to 50,

X is hydroxy, epoxy, vinyl aryl, vinyl, vinyloxy, acrylate, methacrylate or acylchloro or of the formula II ##STR5## wherein Y is N or CH R⁴ is linear or branched C₁ -C₆ alkyl and X is as defined above.

In another embodiment, the aminoquinone of the present invention is copolymerized, preferably to form block, segmented block, or random copolymers, with one or more comonomers reactive with the X group present in the aminoquinone monomer.

In an additional embodiment, the copolymer of the present invention is used to form a binder for magnetic particles in an information storage device.

The aminoquinones of the present invention can be prepared using conventional synthetic methods for reacting amine compounds with quinone. Suitable methods include oxidative amination of benzoquinone (see Torres et al J. Heterocyclic Chem. 23, pp. 697-699 (1985)) and direct amination (see Erhan et al, U.S. Pat. Nos. 4,831,107 and 4,882,413). Particularly preferred is the method of oxidative amination of benzoquinone using calcium hypochlorite as the oxidant.

In the aminoquinone of the present invention, R is preferred to be hydrogen, methyl, ethyl, benzyl, phenethyl, tolyl, xylyl, ethylphenyl, diethylphenyl and (methyl ethyl) phenyl, with hydrogen, methyl and ethyl most preferred.

R¹ is preferred to be linear, branched or cyclic C₁ -C₆ alkylene, phenylene or --CH₂ CH₂ C₆ H₄ --, with the C₁ -C₆ alkylenes being most preferred.

X is a group capable of reacting with comonomer (B) in the copolymer of the present invention, described below. Preferably, X is hydroxy, epoxy, vinyl, vinyloxy, acryl, methacryl or acylchloro, with hydroxy, epoxy and vinyl being most preferred.

A particularly preferred aminoquinone of the present invention is the compound of formula III ##STR6##

The copolymers of the present invention can be prepared by melt or solution polymerization using conventional techniques.

The copolymers are block, segmented block or random copolymers comprising

(A) 3 to 60% by weight, preferably 10-30% by weight, of units derived from one or more reactive aminoquinones of the present invention, and

(B) 40 to 97% by weight, preferably 70-90% by weight, of units derived from one or more comonomers having at least one functional group reactive with the reactive aminoquinone of part (A).

The comonomers (B) are selected to have reactivity with the group X of the aminoquinone, and with each other if a block, or segmented block copolymer is desired. In the present discussion, a block copolymer is a copolymer of general structure -BBBBAAAABBBB- indicating that both the A and B blocks are polymeric, while a segmented block copolymer has a general structure -BBBBABBBB-, indicating that the A block is monomeric or oligomeric (degree of polymerization ≦10) with the B block being polymeric. If (B) comprises more than one type of comonomer, such as diisocyanate and diol in preparation of a polyurethane-aminoquinone copolymer, at least one of the comonomers (B) must be reactive with (A), with the remaining comonomers (B) being reactive with one another.

The copolymers of the present invention are preferably polymers which are conventionally used as binders in magnetic information storage devices, which have been modified by inclusion into the polymer chain of 3 to 30% by weight of units derived from the reactive aminoquinones of the present invention. Suitable comonomers (B) include monomers used in preparing polyurethanes, polyester polyurethanes, poly(vinyl acetate-co-vinyl chloride), epoxy and phenoxy resins, cellulose nitrate, poly(vinylidene bichloride-co-acylonitrile), poly(butadiene-co-styrene), poly(butadiene-co-acrylonitrile), polyamides, poly(vinyl acetal), poly(vinyl butyral), poly(vinyl pyridine) copolymers, polycarbonates, polysulfones, polyimides, polyetherimides, polyether ether ketones, phenol-formaldehyde resins, melamine-formaldehyde resins, poly(acrylate), poly(methacrylate), poly(acrylic acid) and poly(methacrylic acid). Preferred copolymers of the present invention are polyurethane/aminoquinone copolymers, epoxy resin/aminoquinone copolymers, and polyester polyurethane/aminoquinone copolymers, with polyurethane/aminoquinone copolymers and polyester polyurethane/aminoquinone copolymers most preferred.

The copolymer of the present invention has a number average molecular weight of from 1000 to 200,000, preferably from 15,000 to 100,000.

In the preparation of the preferred copolymers of the present invention, when X=OH, the polyurethane constituent of the copolymer can be prepared from one or more comonomers (B) comprising 30 to 50% by weight of a diisocyanate and 30 to 50% by weight of a diol. In particular, preferred diisocyanates have the formula

    O═C═N--R.sup.5 --N═C═O

wherein R⁵ is a linear, branched or cyclic C₂ -C₁₈ aliphatic group, --C₆ H₄ --CH₂ --C₆ H₄ --, or an aryl group which is unsubstituted, or mono or disubstituted by linear, branched or cyclic C₁ -C₆ alkyl, with methylene di-p-phenyldiisocyanate (MDI), diisocyanatotoluene and isophorone diisocyanate and positional isomers thereof being most preferred.

Preferred diols of the polyurethane portion of the copolymer are diols of formula HO--R⁶ --OH wherein R⁶ is a linear, branched or cyclic C₂ -C₁₈ aliphatic group or oligomeric diols. Preferred oligomeric diols include polycaprolactone diol having a degree of polymerization of from 1 to 50, poly(butylene adipate) diol having a degree of polymerization of from 1 to 20, poly(ethylene terephthalate) diol having a degree of polymerization of from 1 to 20, poly(tetrahydrofuran) diol having a degree of polymerization of from 2 to 50, poly(1,2-butylene glycol) diol having a degree of polymerization of from 2 to 50, poly(1,2-propyleneglycol) diol having a degree of polymerization of from 2 to 1000, poly(1,3-propylene glycol) diol having a degree of polymerization of from 2 to 1000, poly(ethylene glycol) diol having a degree of polymerization of from 2 to 1000 and poly(carbonate) diol having a degree of polymerization of from 1 to 20.

When X=vinyl, vinyloxy, acrylate or methacrylate, comonomer (B) is preferably one or more monomers selected from the group consisting of acrylates, methacrylates, C₂ -C₆ olefins, styrene and vinyl naphthalene. When X=epoxy, comonomer (B) is preferably one or more comonomers selected from the group consisting of C₂ -C₄ alkylene oxide, styrene oxide and epichlorohydrin.

In an alternative embodiment, the aminoquinones of the present invention are compounds of the formula (IV): ##STR7## wherein R is as previously described; and R⁷ is --(CH₂)_(n) --, phenyl (--C₆ H₄ --), --C₆ H₄ --O--C₆ H₄ --, --C₆ H₄ --CO--C₆ H₄ --, --C₆ H₄ --SO₂ --C₆ H₄ --, biphenyl, --CH₂ --C₆ H₄ --CH₂ --, 2,5-tolyl-diyl, 2,4-tolyl-diyl, 2,4-anisyl-diyl; wherein n is an integer from 2 to 12, preferably from 2 to 6.

The aminoquinones of formula (IV) may be used to form polyimides for use as a binder in a magnetic information storage device. The polyimides derived from aminoquinones of formula (IV) may prepared by condensation of one or more aminoquinones of formula (IV) with one or more tetracarboxylic dianhydrides. Any tetracarboxylic dianhydride may be used, with dianhydrides of the formulas below: ##STR8## being preferred.

In another embodiment, the aminoquinones of the present invention are compounds of formula (V): ##STR9## wherein R is as previously described; and

R⁸ is --O--(CH₂)_(n) --, phenoxy, phenylsulfonyl or a single bond, wherein n is an integer from 2 to 12, preferably 2 to 6.

The aminoquinones of formula (V) may also be used to prepare polyimides by condensation of one or more aminoquinones of formula (V) with one or more diamines. While any diamine may be used in the preparation of polyimides by condensation with the aminoquinones of formula (V), aromatic diamines are preferred, with 1,4-diaminobenzene, 1,3-diaminobenzene, 4,4'-diamino-diphenyl ether, 4,4'-diamino-benzophenone, 2,4-diaminotoluene, 2,5-diaminotoluene and 4,4'-diamino-diphenyl sulfone being most preferred.

The information storage device of the present invention comprises a support, magnetic particles and a binder to bind the magnetic particles to the support and provide corrosion resistance to the magnetic particles. The binder comprises the copolymer of the present invention described above. In formulating the binder, 30-100% by weight, preferably 40-75% by weight, of the copolymer of the present invention is mixed with one or more conventional binder polymer components used in magnetic particle information storage devices as noted above. Suitable conventional binder components include commercial polyurethanes, polyester polyurethanes and epoxy resins, such as the polyurethane MORTHANE CA-271, commercially available from Morton International.

The information storage device of the present invention can be prepared by conventional methods, such as those described in the chapter entitled "Magnetic Tape" from Kirk-Othmer Encyclopedia of Chemical Technology and the references cited therein. A key difference between the device of the present invention and conventional devices is the use of the aminoquinone-containing copolymer of the present invention as the binder in the device. The device may be any magnetic information storage device which requires the use of magnetic particles, which would be susceptible to corrosion. Preferred devices include magnetooptic discs and magnetic particle tape.

The magnetic particles present in the device of the present invention may be any conventional magnetic particles used in information storage media. For magnetic particle tape, Fe particles or alloys such as iron nitrides are preferred. For thin film media prepared by vapor deposition of the metal on the medium, Co and Fe/Co alloys are preferred in recording heads and Fe/Gd alloys and Fe/Yb/Co alloys are preferred in magnetooptic discs.

By using the aminoquinone-containing copolymers of the present invention as binders in magnetic particle information storage devices, improved corrosion resistance is obtained while maintaining or improving the mechanical properties of the device.

Having generally described this invention, a further understanding can be obtained by reference to certain specific examples which are provided herein for purposes of illustration only and are not intended to be limiting unless otherwise specified.

EXAMPLES Example 1

Preparation of the amine-quinone monomer 2,5-bis(N-2-hydroxyethyl-N-methylamino)-1,4-benzoquinone (AQM-1). A 500 mL, three-necked, round bottom flask was equipped with a mechanical stirrer, a reflux condenser, and a dropping funnel. Tetrahydrofuran (300 mL) was added to the flask, cooled to 5° C. Powdered calcium hypochlorite (22.8 g, 0.160 mol) was added to the tetrahydrofuran and the suspension was stirred for 10 minutes. To this suspension was added benzyltrimethylammonium chloride (0.74 g, 4.0 mmol), followed by 1,4-benzoquinone (17.30 g, 0.1600 mol). A solution of N-(2-methylamino)ethanol (24.04 g, 0.3200 mol, dissolved in 100 ml of THF) was added dropwise over a period of 40 minutes. After the addition of N-(2-methylamino)ethanol, the reaction mixture was stirred for 1.5 hours and then heated at 40° C. for 1 hour. After cooling to room temperature, the reaction mixture was filtered through Spectra/Mesh® polypropylene filter (500 μm mesh opening, supplied by Spectrum Medical Industries, Inc) to remove the calcium hypochlorite particles. Fine particles of the crude product were recovered from the filtrates by filtration through sintered glass funnel. Boiling ethanol was poured into the filtration funnel to extract amine-quinone monomer. This ethanol solution was then filtered through the funnel by suction. A 450 ml solution was collected after repeated extraction. After cooling the solution overnight in a refrigerator at 4° C. the product crystallized. The crystals were collected by filtration and further purified by a second extractive recrystallization from ethanol (yield 76%, m.p. 167° C). The product consisted of fine orange-brown needles with a purple cast in reflection. Elemental analysis: found C 56.70%, H 7.19%, N 11.03%, calculated for C₁₂ H₁₆ N₂ O₄, C 56.68%, H 7.13%, N 11.02%. ¹ H NMR(CD₃ SOCD₃): 3.1 ppm (s, CH₃ N, 6H), 3.5-3.6 ppm (q, CH₂ N, 4H), 3.7-3.8 ppm (t, CH₂ O, 4H), 4.7-4.8 ppm (t, --OH, 2H), 5.28 ppm (s, quinone-H, 2H). Exact mass by mass spectroscopy 254.13, calculated 254.29.

Example 2

Preparation of the amine-quinone monomer 2,5-bis[4-(2hydroxyethyl)piperazinyl]-1,4-benoquinone (AQM-2). A 500 mL, three-necked, round bottom flask was equipped with a mechanical stirrer, a reflux condenser, and a dropping PG,18 funnel. Tetrahydrofuran (300 mL) was added to the flask and cooled to 5° C. Powdered calcium hypochlorite (22.8 g, 0.160 mole) was added to the tetrahydrofuran and the suspension was stirred for 10 minutes. To this solution was added benzyltrimethylammonium chloride (0.74 g, 4.0 mmol), followed by 1,4-benzoquinone (17.30 g, 0.1600 mole). A solution of 1-(2-hydroxyethyl)piperazine (41.66 g, 0.3200 mole, dissolved in 100 ml of THF) was added dropwise over a period of 40 minutes. After the addition of 1-(2-hydroxyethyl)piperazine, the reaction mixture was stirred for 1.5 hours and then heated at 40° C. for 1 hour. After cooling to room temperature, the reaction mixture was filtered through Spectra/Mesh® polypropylene filter to remove the calcium hypochlorite particles. Fine particles of the crude product were recovered from the filtrates by filtration through sintered glass funnel. Boiling ethanol was poured into the filtration funnel to extract aminequinone monomer. This ethanol solution was then filtered through the funnel by suction. A 450 ml amine-quinone ethanol solution was collected after repeated extraction. The product was crystallized after cooling the solution overnight in a refrigerator at 4° C. The crystals were then collected by filtration and further purified by a second extractive recrystallization from ethanol (yield 66%, m.p. 165° C). The product consisted of fine red crystals.

Example 3

Synthesis of Amine-Quinone Polyurethane AQPU-2. Polycaprolactone diol (25 g, 0.02 mole) was dehydrated in three-necked flask by stirring at 100° C under reduced pressure for 30 minutes, and then cooled to 60° C. The polycaprolactone diol was vigorously mixed with AQM-1 (1 g, 0.004 mol) for 1 hour at 85° C. Methylene di-p-phenyldiisocyanate (MDI) (6.17 g, 0.025 mol) was added to the flask under nitrogen. The mixture was vigorously mixed for one minute. One drop of stannous 2-ethylhexanoate at 60° C. was added to the flask and mixed for 30 second, followed by degassing under reduced pressure for one minute. The reaction mixture was poured into a beaker before being cured in oven at 80° C under vacuum. The number average molecular weight M_(n) was determined by gel permeation chromatography to be 43,400.

Example 4

Synthesis of an Amine-Quinone Polyurethane, AQPU-3. The required amount of polycaprolactone diol (5 g, 0.004 mole) was dehydrated in three-necked flask by stirring at 100° C under reduced pressure for 30 minutes, and then cooled to 40° C. The corresponding amount of isophorone diisocyanate (IPDI) (1.798 g, 0.008 mole) was dissolved in THF and was added into the flask under nitrogen. The final concentration of the polycaprolactone diol and the IPDI was 10% (w/v). The mixture was refluxed gently for 1 hour and cooled to 40° C. The corresponding amount of AQM-1 (0.75 g, 0.003 mole) was added into the prepolymer solution, followed by three drops of stannous 2-ethylhexanoate. The mixture was refluxed for 3 hours, with constant stirring. The resultant polymer was precipitated from excess methanol before being stored overnight. The precipitate was isolated by filtering and extensively washed with methanol. It was then dried in vacuum at 60° C. The number average molecular weight M_(n) was determined by gel permeation chromatography to be 14,860.

Example 5

synthesis of an Amine-Quinone Polyurethane, AQPU-4. The required amount of polycaprolactone diol (5 g, 0,004 mole) was dehydrated in three-necked flask by stirring at 100° C under reduced pressure for 30 minutes, and then cooled to 40° C. The corresponding amount of IPDI (2.59 g, 0.0116 mole) was dissolved in THF and was added into the flask under nitrogen. The final concentration of the polycaprolactone diol and the IPDI was 10% (w/v). The mixture was refluxed gently for i hour and cooled to 40° C. The corresponding amount of AQM-1 (1.75 g, 0,007 mole) was added into the prepolymer solution, followed by three drops of stannous 2-ethylhexanoate. The mixture was refluxed for 3 hours, with constant stirring. The resultant polymer was precipitated from excess methanol before being stored overnight. The precipitate was isolated by filtering and extensively washed with methanol. It was then dried in vacuum at 60° C. The number average molecular weight M_(n) was determined by gel permeation chromatography to be 11,400.

Example 6

Synthesis of an Amine-Quinone Polyurethane, AQPU-8. The required amount of poly(1,2-butylene glycol) (5 g, 0.0025 mole) was dehydrated in three-necked flask by stirring at 100° C. under reduced pressure for 30 minutes, and then cooled to 40° C. The corresponding amount of tolylene-2,4-diisocyanate (TDI) (1.72 g, 0.0098 mole) was dissolved in dimethyl formamide (DMF) and was added into the flask under nitrogen. The final concentration of the poly(1,2-butylene glycol) and TDI was 10% (w/v). The mixture was stirred gently at 80° C. for 2 hours and cooled to 40° C. The corresponding amount of AQM-1 (1.75 g, 0.007 mole) was added into the prepolymer solution, followed by three drops of stannous 2-ethylhexanoate. The mixture was stirred at 90° C. for 3 hours, with constant stirring. The resultant polymer was precipitated from excess methanol before being stored overnight. The precipitate was isolated by filtering and extensively washed with methanol. It was then dried in vacuum at 60° C. This composition contained 20.7 weight percent AQM-1. This polymer was completely soluble in tetrahydrofuran, toluene, and cyclohexanone. The number average molecular weight, by GPC, was 89,300.

Example 7

Synthesis of an Amine-Quinone Polyurethane, AQPU-10. The required amount of poly(1,2-butylene glycol) (5 g, 0.0025 mole) was dehydrated in three-necked flask by stirring at 100° C. under reduced pressure for 30 minutes, and then cooled to 40° C. The corresponding amount of MDI (2.46 g, 0.0098 mole) was dissolved in dimethyl formamide (DMF) and was added into the flask under nitrogen. The final concentration of the poly(1,2-butylene glycol) and MDI was 10% (w/v). The mixture was stirred gently at 80° C. for 2 hours and cooled to 40° C. The corresponding amount of AQM-1 (1.75 g, 0,007 mole) was added into the prepolymer solution, followed by three drops of stannous 2-ethylhexanoate. The mixture was stirred at 90° C. for 4 hours, with constant stirring. The resultant polymer was precipitated from excess methanol before being stored overnight. The precipitate was isolated by filtering and extensively washed with methanol. It was then dried in vacuum at 60° C. This composition contained 20 weight percent AQM-1. This polymer was completely soluble in tetrahydrofuran, toluene, and cyclohexanone. The number average molecular weight, by GPC, was 81,100.

Example 8

Synthesis of an Amine-Quinone Polyurethane, AQPU-11. The required amount of poly(1,2-butylene glycol) (5 g, 0.0025 mole) was dehydrated in three-necked flask by stirring at 100° C. under reduced pressure for 30 minutes, and then cooled to 40° C. The corresponding amount of MDI (1,927 g, 0.0077 mole) was dissolved in dimethyl formamide (DMF) and was added into the flask under nitrogen. The final concentration of the poly(1,2-butylene glycol) and MDI was 10% (w/v). The mixture was stirred gently at 80° C. for 2 hours and cooled to 40° C. The corresponding amount of AQM-2 (1.75 g, 0.0048 mole) was added into the prepolymer solution, followed by three drops of stannous 2-ethylhexanoate. The mixture was stirred at 90° C. for 4 hours, with constant stirring. The resultant polymer was precipitated from excess methanol before being stored overnight. The precipitate was isolated by filtering and extensively washed with methanol. It was then dried in vacuum at 60° C. This composition contained 20.2 weight percent AQM-2. This polymer was completely soluble in tetrahydrofuran, toluene, and cyclohexanone. This polyurethane has better thermal stability in air. It has only 3% weight loss at 255° C.

Example 9

Films Containing Amine-Quinone Polyurethane, AQPU-8, and Iron Pigments. Two different binder polymer solutions were prepared: 1) a wetting binder solution contained 1.84 g of AQPU-8, 16.03 g tetrahydrofuran, 16.52 g of cyclohexanone, and 1.76 g toluene; and 2) a binder solution contained 2.33 g of MORTHANE CA-271 (a commercial polyurethane binder from Morton International), 2.63 g tetrahydrofuran, 5.21 g cyclohexanone, and 5.24 g toluene. Both solutions were continuously mixed on the wrist-action shaker overnight to effect dissolution of the polymers. The next day the polymer solutions were used to prepare a magnetic coating dispersion. To a 150 mL beaker was added 16.82 g of iron pigments (a generic iron pigment used in the preparation of commercial metal particle magnetic tape) and the wetting binder solution. The mixture was thoroughly stirred in order to completely wet the iron pigments. The slurry was charged to an Eiger Mini 50 mill, 25.42 g of cyclohexanone was added, and the mill was started at full speed. After ten minutes milling, a mixture of 0.33 g carbon black, 1.07 g alumina, 0.23 g stearic acid, and 0.23 g butyl stearate was added to the mill. While the milling continued, 0.46 g MONDUR CB-701 (a commercial Polyisocyanate crosslinker from Mobay Coatings Division) was dissolved in the MORTHANE CA-271 binder solution. After 50 minutes milling, the MORTHANE solution was added to the mill and the milling was continued for ten more minutes. After a total of one hour of milling the dispersion was discharged into a glass bottle and ready for coating trials.

Films were coated onto 3 mil thick polyester base film by hand-drawing using a Gardner Blade. Immediately after coating the films were longitudinally oriented in a 2000 gauss magnetic field. The films were dried overnight in a convection oven at 60° C.

Example 10

Films Containing Amine-Quinone Polyurethane, AQPU-4, and Iron Pigments. Two different binder polymer solutions were prepared: 1) a wetting binder solution contained 1.81 g of AQPU-4, 16.64 g tetrahydrofuran, 16.46 g of cyclohexanone, and 4.23 g toluene; and 2) a binder solution contained 2.37 g of MORTHANE CA-271 (a commercial polyurethane binder from Morton International), 2.79 g tetrahydrofuran, 5.24 g cyclohexanone, and 5.32 g toluene. Both solutions were continuously mixed on the wrist-action shaker overnight to effect dissolution of the polymers. The next day the polymer solutions were used to prepare a magnetic coating dispersion. To a 150 mL beaker was added 16.82 g of iron pigments (a generic iron pigment used in the preparation of commercial metal particle magnetic tape) and the wetting binder solution. The mixture was thoroughly stirred in order to completely wet the iron pigments. The slurry was charged to an Eiger Mini 50 mill, 25.42 g of cyclohexanone was added, and the mill was started at full speed. After ten minutes milling, a mixture of 0.33 g carbon black, 1.07 g alumina, 0.23 g stearic acid, and 0.23 g butyl stearate was added to the mill. While the milling continued, 0.46 g MONDUR CB-701 (a commercial polyisocyanate crosslinker from Mobay Coatings Division) was dissolved in the MORTHANE CA-271 binder solution. After 50 minutes milling, the MORTHANE solution was added to the mill and the milling was continued for ten more minutes. After a total of one hour of milling the dispersion was discharged into a glass bottle and ready for coating trials.

Films were coated onto 3 mil thick polyester base film by hand-drawing using a Gardner Blade. Immediately after coating the films were longitudinally oriented in a 2000 gauss magnetic field. The films were dried overnight in a convection oven at 60° C.

Comparative Example 1

Films Containing a Conventional Metal Particle Formulation. A conventional metal particle tape formulation was used to prepare films for comparison with the films containing amine-quinone polymers. Two different binder polymer solutions were prepared: 1) a wetting binder solution containing 3.75 g UCARMAG-536 (a commercial wetting binder from Union Carbide Corporation), 3.50 g cyclohexanone, 1.75 g tetrahydrofuran, and 3.50 g toluene; and 2) a binder solution containing 4.58 g MORTHANE CA-271, 10.39 g cyclohexanone, 5.19 g tetrahydrofuran, and 10.39 g toluene. Both solutions were mixed overnight on a wrist-action shaker to effect dissolution of the polymers. The next day the polymer solutions were used to prepare a magnetic coating dispersion. To a 150 mL beaker was added 33.33 g of iron pigment and the wetting binder solution. The mixture was thoroughly stirred in order to completely wet the iron pigments. Then 0.67 g carbon black, 2.00 g alumina, 20.60 g cyclohexanone, 10.30 g tetrahydrofuran, 20.60 g toluene, and 0.42 g butyl stearate were added to the mixture. The slurry was charged to an Eiger Mini 50 mill and was milled at full speed. While the milling continued, 1.19 g MONDUR CB-701 (a commercial polyisocyanate crosslinker from Mobay Coatings Division) was dissolved in the MORTHANE CA-271 binder solution. After 50 minutes milling, the MORTHANE solution was added to the mill and the milling was continued for ten more minutes. After a total of one hour of milling the dispersion was discharged into a glass bottle and ready for coating trials.

Films were coated onto 3 mil thick polyester base film by hand-drawing using a Gardner Blade. Immediately after coating the films were longitudinally oriented in a 2000 gauss magnetic field. The films were dried overnight in a convection oven at 60° C.

Comparative Example 2

Preparation of an Amine-Quinone Polymer Containing Jeffamine D400 and p-Benzoquinone (COMP-1). For the purposes of comparison a sample of amine-quinone polymer was prepared exactly as described in example 1 of Erhan U.S. Pat. 4,882,413. A 250 mL round bottom flask was charged with solution of Jeffamine D400 (16.0 g, 0.0400 mol) in 50 mL ethanol. A solution of 6.48 g (0.0600 mol) p-benzoquinone in 50 ml ethanol was added to the flask and the flask was equipped with a reflux condenser and magnetic stirring. The mixture was refluxed over a water bath for 3 hr. After 3 hr the ethanol was removed on a rotary evaporator. The residue was a viscous syrup. It was washed with cold water. The residue was dissolved in acetone, and then precipitated in hot water. The polymer was repeatedly washed with hot water until the wash water was colorless (about 5 liters of water was used). The residue was dried in a vacuum oven at 50° C. for 5 hr.

Comparative Example 3

Films Containing COMP-1 and Iron Particles. Two different binder polymer solutions were prepared: 1) a wetting binder solution contained 1.80 g of COMP-1, 16.04 g tetrahydrofuran, and 4.02 g of cyclohexanone; and 2) a binder solution contained 2.33 g of MORTHANE CA-271 (a commercial polyurethane binder from Morton International), 2.66 g tetrahydrofuran, 5.21 g cyclohexanone, and 5.26 g toluene. Both solutions were continuously mixed on the wrist-action shaker overnight to effect dissolution of the polymers. The next day the polymer solutions were used to prepare a magnetic coating dispersion. To a 150 mL beaker was added 12.02 g cyclohexanone, 1.90 g toluene, 16.82 g of iron pigments and the wetting binder solution. The mixture was thoroughly stirred in order to completely wet the iron pigments. The slurry was charged to an Eiger Mini 50 mill, 25.42 g of cyclohexanone was added, and the mill was started at full speed. After the mixture had milled for 5 min, a mixture of 0.40 g carbon black in 25.33 g tetrahydrofuran was added to the mill. After 20 min milling, a mixture of 1.15 g alumina, 0.35 g stearic acid, and 0.23 g butyl stearate was added to the mill. While the milling continued, 0.45 g MONDUR CB-701 was dissolved in the MORTHANE CA-271 binder solution. After 55 minutes milling, the MORTHANE solution was added to the mill and the milling was continued for 5 min more. After a total of one hour of milling the dispersion was discharged into a glass bottle and ready for coating trials.

Films were coated onto 3 mil thick polyester base film by hand-drawing using a Gardner Blade. Immediately after coating the films were longitudinally oriented in a 2000 gauss magnetic field. The films were dried overnight in a convection oven at 60° C.

Comparative Corrosion Studies

To demonstrate the effect of corrosion inhibition for the amine-quinone polymers of the present invention, comparative corrosion studies were undertaken. Circular samples with a 6 mm diameter were punched from the films. Magnetic hysteresis loops were measured by vibrating sample magnetometry with the applied field parallel to the direction of orientation. Initial values of saturation magnetization (MS) were obtained for each sample. The samples were soaked in pH 2.00 aqueous buffer for a period of time, removed, another hysteresis loop measured and then returned to the buffer solution. The result was a data set consisting of saturation magnetization as a function of time exposed to pH 2.00 buffer. For each sample the relative saturation magnetization was determined by dividing the values of saturation magnetization by the initial value of saturation magnetization. FIG. 1 shows a plot of the relative saturation magnetization as a function of time exposed to the buffer. When exposed to aqueous acid, iron metal corrodes according to equation 1.

    Fe+2H.sup.+ →Fe.sup.2+ +H.sub.2                     (1)

As the acid penetrated into the samples and corroded the iron particles, the saturation magnetization would decrease. In FIG. 1 the two comparative examples showed a decrease in saturation magnetization, indicating extensive corrosion. However, the three examples, two replicate AQPU-8 samples and one AQPU-4 sample, showed no significant decrease in saturation magnetization. This demonstrates that the amine-quinone polyurethane binders give a great improvement in the corrosion resistance for metal particles over a conventional metal particle binder formulations. Further more the data demonstrates that the polymers disclosed by Erhan provide no increase in corrosion protection relative to the generic metal particle binder formulations, whereas the polymers of the present invention provide a remarkable increase in corrosion protection.

Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein. 

What is claimed as new and desired to be secured by Letters Patent of the United States is:
 1. A copolymer comprising(A) 3 to 60% by weight, of units derived from one or more reactive aminoquinones of formula I ##STR10## wherein R is hydrogen, branched, linear or cyclic C₁ -C₆ alkyl, aralkyl, or phenyl which may be substituted by linear, branched or cyclic C₁ -C₄ alkyl, --NO₂, F, OR², NR³ ₂, wherein R² and R³ are linear, branched or cyclic C₁ -C₆ alkyl, aralkyl or phenyl, R¹ is a linear, branched or cyclic C₂ -C₁₈ alkylene chain, phenylene, aralkylene, alkarylene, or --(CH₂ CH₂ --O)_(n) --CH₂ --CH₂ --, wherein n is an integer from 1 to 50, X is hydroxy, epoxy, vinyl, vinyloxy, acrylate, methacrylate or acylchloro or of the formula II ##STR11## wherein Y is N or CH R⁴ is linear or branched C₁ -C₆ alkyl and X is as defined above, and (B) 40 to 97% by weight, of units derived from one or more comonomers having at least one functional group reactive with the reactive aminoquinone of part (A).
 2. The copolymer of claim 1 wherein said copolymer comprises 10 to 30% by weight of (A) and 70 to 90% by weight of (B).
 3. The copolymer of claim 1 wherein X is OH and said one or more comonomers (B) comprises30 to 50% of a diisocyanate and 30 to 50% of a diol.
 4. The copolymer of claim 3 wherein said diisocyanate has the formula

    O═C═N--R.sup.5 --N═C═O

wherein R⁵ is a linear, branched or cyclic C₂ -C₁₈ aliphatic group, --C₆ H₄ --CH₂ --C₆ H₄ --, or an aryl group which is unsubstituted, or mono or disubstituted by linear, branched or cyclic C₁ -C₆ alkyl.
 5. The copolymer of claim 4 wherein said diisocyanate is a member selected from the group consisting of methylene di-p-phenyldiisocyanate, diisocyanatotoluene, isophorone diisocyanate and positional isomers thereof.
 6. The copolymer of claim 3 wherein said diol is a diol of formula HO--R⁶ --OH wherein R⁶ is a linear, branched or cyclic C₂ -C₁₈ aliphatic group or said diol is an oligomeric diol selected from the group consisting of polycaprolactone diol having a degree of polymerization of from 1 to 50, poly(butylene adipate) diol having a degree of polymerization of from 1 to 20, poly(ethylene terephthalate) diol having a degree of polymerization of from 1 to 20, poly(tetrahydrofuran) diol having a degree of polymerization of from 2 to 50, poly(1,2-butylene glycol) diol having a degree of polymerization of from 2 to 50, poly(1,2-propyleneglycol) diol having a degree of polymerization of from 2 to 1000, poly(1,3-propylene glycol) diol having a degree of polymerization of from 2 to 1000, poly(ethylene glycol) diol having a degree of polymerization of from 2 to 1000 and poly(carbonate) diol having a degree of polymerization of from 1 to
 20. 7. The copolymer of claim 1 wherein X is vinyl, vinyloxy, acrylate or methacrylate and (B) is one or more monomers selected from the group consisting of acrylates, methacrylates, C₂ -C₆ olefins, styrene and vinyl naphthalene.
 8. The copolymer of claim 1 wherein X is epoxy and (B) is one or more comonomers selected from the group consisting of C₂ -C₄ alkylene oxide, styrene oxide and epichlorohydrin.
 9. A copolymer comprising units derived from(A) one or more reactive aminoquinones of formula (IV): ##STR12## wherein R is hydrogen, branched, linear or cyclic C₁ -C₆ alkyl, aralkyl, or phenyl which may be substituted by linear, branched or cyclic C₁ -C₄ alkyl, --NO₂, F, OR², NR³ ₂, wherein R² and R³ are linear, branched or cyclic C₁ -C₆ alkyl, aralkyl or phenyl; and R⁷ is --(CH₂)_(n) --, phenyl (--C₆ H₄ --), --C₆ H₄ --O--C₆ H₄ --, --C₆ H₄ --CO--C₆ H₄ --, --C₆ H₄ --SO₂ --C₆ H₄ --, biphenyl, --CH₂ --C₆ H₄ --CH₂ --, 2,5-tolyl-diyl, 2,4-tolyl-diyl or 2,4-anisyl-diyl; wherein n is an integer from 2 to 12; and (B) one or more tetracarboxylic dianhydrides.
 10. The copolymer of claim 9, wherein said tetracarboxylic dianhydrides are one or more members selected from the group of compounds of formulas: ##STR13##
 11. A copolymer comprising units derived from(A) one or more reactive aminoquinones of formula (V): ##STR14## wherein R is hydrogen, branched, linear or cyclic C₁ -C₆ alkyl, aralkyl, or phenyl which may be substituted by linear, branched or cyclic C₁ -C₄ alkyl, --NO₂, F, OR², NR³ ₂, wherein R² and R³ are linear, branched or cyclic C₁ -C₆ alkyl, aralkyl or phenyl; and R⁸ is --O--(CH₂)_(n) --, phenoxy, phenylsulfonyl or a single bond, wherein n is an integer from 2 to 12; and (B) one or more diamines.
 12. The copolymer of claim 11, wherein said diamines are one or more members selected from the group consisting of 1,4-diaminobenzene, 1,3-diaminobenzene, 4,4'-diamino-diphenyl ether, 4,4'-diamino-benzophenone, 2,4-diaminotoluene, 2,5-diaminotoluene and 4,4'-diaminodiphenyl sulfone. 